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330-80-3

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330-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 330-80-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 330-80:
(5*3)+(4*3)+(3*0)+(2*8)+(1*0)=43
43 % 10 = 3
So 330-80-3 is a valid CAS Registry Number.

330-80-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-fluoro-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names 2-Fluor-3-phenyl-propionsaeure-ethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:330-80-3 SDS

330-80-3Relevant articles and documents

Enantioselective Suzuki cross-couplings of unactivated 1-fluoro-1-haloalkanes: Synthesis of chiral β-, γ-, δ-, and ε-fluoroalkanes

Jiang, Xiaojian,Gandelman, Mark

supporting information, p. 2542 - 2547 (2015/03/04)

The incorporation of fluorine atom into a stereogenic center is a highly challenging transformation with current methodologies offering access mainly to chiral α- and β-fluoroalkanes. In this article, the development of a novel general approach to constru

Efficient synthesis of secondary alkyl fluorides via suzuki cross-coupling reaction of 1-halo-1-fluoroalkanes

Jiang, Xiaojian,Sakthivel, Sekarpandi,Kulbitski, Kseniya,Nisnevich, Gennady,Gandelman, Mark

supporting information, p. 9548 - 9551 (2014/07/22)

Organofluorine compounds have found extensive applications in various areas of science. Consequently, the development of new efficient and selective methods for their synthesis is an important goal in organic chemistry. Here, we present the first Suzuki c

Simple procedure for preparation of α-fluoro esters by fluorination of ester enol silyl ethers with perchloryl fluoride

Fujisawa, Hidehito,Takeuchi, Yoshio

, p. 173 - 176 (2007/10/03)

Fluorination of ester enol silyl ethers in THF at room temperature using diluted perchloryl fluoride (FClO3) in the presence of ca. 0.5M eq. of t-BuNH2 as an additive produced the corresponding α-fluoro esters in over 80% yields.

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